UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000022786
Receipt number R000026266
Scientific Title Investigation of airway method for extremely emergent cesarean section
Date of disclosure of the study information 2016/06/19
Last modified on 2019/06/22 21:41:06

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Investigation of airway method for extremely emergent cesarean section

Acronym

Investigation of airway method for extremely emergent cesarean section

Scientific Title

Investigation of airway method for extremely emergent cesarean section

Scientific Title:Acronym

Investigation of airway method for extremely emergent cesarean section

Region

Japan


Condition

Condition

extremely emergent cesarean section

Classification by specialty

Obstetrics and Gynecology Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Investigation of airway method for extremely emergent cesarean section

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Airway method

Key secondary outcomes

postoperative pneumonia


Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit


Not applicable

Age-upper limit


Not applicable

Gender

Female

Key inclusion criteria

extremely emergent cesarean section

Key exclusion criteria

none

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Hironobu
Middle name
Last name Ueshima

Organization

Showa University Hospital

Division name

Anesthesiology

Zip code

142-8666

Address

1-5-8 Hatanodai, Shinagawa-ku, Tokyo, Japan

TEL

03-3784-8575

Email

ueshimhi@yahoo.co.jp


Public contact

Name of contact person

1st name Hironobu
Middle name
Last name Ueshima

Organization

Showa University Hospitalhowa

Division name

Anesthesiology

Zip code

142-8666

Address

1-5-8 Hatanodai, Shinagawa-ku, Tokyo, Japan

TEL

03-3784-8575

Homepage URL


Email

ueshimhi@yahoo.co.jp


Sponsor or person

Institute

Showa University Hospital

Institute

Department

Personal name



Funding Source

Organization

Showa University Hospital

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Showa university hospital

Address

1-5-8, hatanodai, shinagawa-ku, tokyo

Tel

03-3784-8575

Email

ueshimhi@med.showa-u.ac..jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2016 Year 06 Month 19 Day


Related information

URL releasing protocol

file:///Users/UESHIMAHIRONOBU/Desktop.htm

Publication of results

Published


Result

URL related to results and publications

file:///Users/UESHIMAHIRONOBU/Desktop.htm

Number of participants that the trial has enrolled

200

Results

Safety

Results date posted

2019 Year 06 Month 22 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics

pregnancy

Participant flow

general anesthesia

Adverse events

none

Outcome measures

safety

Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2016 Year 06 Month 19 Day

Date of IRB

2016 Year 06 Month 19 Day

Anticipated trial start date

2016 Year 06 Month 19 Day

Last follow-up date

2016 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Survey time is from January 2014 to December 2015.
Investigation items are airway method and postoperative pneumonia.


Management information

Registered date

2016 Year 06 Month 19 Day

Last modified on

2019 Year 06 Month 22 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000026266


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name